SLC34A3 mutations in patients with hereditary hypophosphatemic rickets with hypercalciuria predict a key role for the sodium-phosphate cotransporter NaPi-IIc in maintaining phospha... von Bergwitz, Clemens, Roslin, Nicole M, Tieder, Martin, Loredo-Osti, J C, Bastepe, Murat, Abu-Zahra, Hilal, Frappier, Danielle, Burkett, Kelly, Carpenter, Thomas O, Anderson, Donald, Garabedian, Michele, Sermet, Isabelle, Fujiwara, T Mary, Morgan, Kenneth, Tenenhouse, Harriet S, Juppner, Harald

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Patient Characteristics Associated with Differences in Admission Frequency for Diabetic Ketoacidosis in United States Children's Hospitals von Malik, Faisal S., MD, MS, Hall, Matt, PhD, Mangione-Smith, Rita, MD, MPH, Keren, Ron, MD, MPH, Mahant, Sanjay, MD, MSc, Shah, Samir S., MD, MSCE, Srivastava, Rajendu, MD, MPH, Wilson, Karen M., MD, MPH, Tieder, Joel S., MD, MPH

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Management of Apparent Life-Threatening Events in Infants: A Systematic Review von Tieder, Joel S., MD, MPH, Altman, Robin L., MD, Bonkowsky, Joshua L., MD, PhD, Brand, Donald A., PhD, Claudius, Ilene, MD, Cunningham, Diana J., MLS, MPH, AHIP, DeWolfe, Craig, MD, Med, Percelay, Jack M., MD, MPH, Pitetti, Raymond D., MD, MPH, Smith, Michael B.H., MB, FRCPC, FRCPCH

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Hereditary hypophosphatemic rickets with hypercalciuria is not caused by mutations in the Na/Pi cotransporter NPT2 gene von JONES, Andrew O, TZENOVA, Jordana, RICE, Allan, ANDERSON, Donald, MORGAN, Kenneth, FUJIWARA, T. Mary, TENENHOUSE, Harriet S, FRAPPIER, Danielle, CRUMLEY, M. Joyce, ROSLIN, Nicole M, KOS, Claudine H, TIEDER, Martin, LANGMAN, Craig B, PROESMANS, Willem, CARPENTER, Thomas O

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The Weismann-Netter, Stuhl syndrome : a rare pediatric skeletal dysplasia von TIEDER, M, MANOR, H, PESHIN, J, ALON, U. S

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Variation in Inpatient Resource Utilization and Management of Apparent Life-Threatening Events von Tieder, Joel S., MD, MPH, Cowan, Charles A., MD, Garrison, Michelle M., PHD, Christakis, Dimitri A., MPH

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SLC34A3 Mutations in Patients with Hereditary Hypophosphatemic Rickets with Hypercalciuria Predict a Key Role for the Sodium-Phosphate Cotransporter NaP sub(i)-IIc in Maintaining P... von Bergwitz, C, Roslin, N M, Tieder, M, Loredo-Osti, J C, Bastepe, M, Abu-Zahra, H, Frappier, D, Burkett, K, Carpenter, TO, Anderson, D, Garabedian, M, Sermet, I, Fujiwara, T M, Morgan, K

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Quality Improvement Research in Pediatric Hospital Medicine and the Role of the Pediatric Research in Inpatient Settings (PRIS) Network von Simon, Tamara D., MD, MSPH, Starmer, Amy J., MD, MPH, Conway, Patrick H., MD, MSc, Landrigan, Christopher P., MD, MPH, Shah, Samir S., MD, MSCE, Shen, Mark W., MD, Sectish, Theodore C., MD, Spector, Nancy D., MD, Tieder, Joel S., MD, MPH, Srivastava, Rajendu, MD, FRCP(C), MPH, Willis, Leah E., MS, Wilson, Karen M., MD, MPH

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Hypophosphataemic rickets and final height von Stamp, Trevor, Goldstein, A.J., Balsan, S., Tieder, M.

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Spondyloepiphyseal dysplasia associated with progressive arthropathy. An unusual disorder mimicking juvenile rheumatoid arthritis von Robinson, D, Tieder, M, Halperin, N, Copeliovitch, L

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Hypercalciuria as a cause of persistent or recurrent haematuria von Stark, H, Tieder, M, Eisenstein, B, Davidovits, M, Litwin, A

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Linear growth in patients with hypophosphatemic vitamin D-resistant rickets: Influence of treatment regimen and parental height von Balsan, Sonia, Tieder, Martin

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Maffucci's syndrome—The result of neural abnormalities? Evidence of mitogenic neurotransmitters present in enchondromas and soft tissue hemangiomas von Robinson, Dror, Tieder, Martin, Halperin, Nahum, Burshtein, David, Nevo, Zvi

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Thirty years of innovation in foster care von Tieder, M

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Multiple exostoses ― mental retardation syndrome: a case report and review of the literature von MIROVSKY, Y, HALPERIN, N, COPELIOVITCH, L, TIEDER, M

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Hereditary Hypophosphatemic Rickets with Hypercalciuria von Tieder, Martin, Modai, David, Samuel, Ruth, Arie, Raphael, Halabe, Aharon, Bab, Itai, Gabizon, Daniela, Liberman, Uri A

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A practical approach to the treatment of burn shock in childhood von Vure, E., Joseph, M., Beer, S., Tieder, M., Krespin, H., Taunus, A., Shulman, J.

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Mental retardation with 45 chromosomes 45,XX,--5,--14,+der(5) t(5,14)(p15;q13) mat due to familial balanced reciprocal translocation von Fried, K, Tieder, M, Beer, S, Rosenblatt, M, Krespin, H I

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Trisomy 13 Mosaic Presenting as Cleft Lip and Palate von Beer, S., Fried, K., Krespin, H. I., Rosenblatt, M., Tieder, M.

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Elevated Serum 1,25-Dihydroxyvitamin D Concentrations in Siblings with Primary Fanconi's Syndrome von Tieder, Martin, Arie, Raphael, Modai, David, Samuel, Ruth, Weissgarten, Joshua, Liberman, Uri A

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